Canonical Allele Identifier: PA916056490
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 280278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Glu123Asp
CA6798547
NM_080601.3:c.369G>T
CA386780704
NM_080601.3:c.369G>C